AI Article Synopsis

  • - The study aimed to assess the feasibility and acceptability of a smartphone app designed to enhance adherence to positive airway pressure (PAP) therapy among patients newly diagnosed with obstructive sleep apnea (OSA).
  • - In a randomized controlled trial involving 87 participants, researchers measured app engagement, retention rates, and patient feedback to evaluate the app's effectiveness compared to standard care and activity monitoring.
  • - Results showed that the app was both feasible and acceptable, with high PAP usage reported in both groups, but no significant differences in adherence or clinical outcomes were found between the app users and the control group.

Article Abstract

Objective: To investigate the feasibility and acceptability of , a multicomponent, evidence-based smartphone application, to improve positive airway pressure therapy (PAP) adherence, among patients with obstructive sleep apnea (OSA) naive to PAP.

Methods: In a single-blind randomized controlled trial, , with a companion activity monitor was compared to usual care plus the activity monitor and its associated app. provides objective feedback on PAP usage and sleep/physical activity patterns, and chronic disease management. Patients were recruited from two sleep medicine centers and followed over the first 60 days of PAP. Feasibility and acceptability were measured by recruitment/retention rates, app usage, differences in post-trial Treatment Evaluation Questionnaire (TEQ) scores, and patient interviews. Exploratory, intent-to-treat logistic and linear mixed models estimated PAP adherence and clinical outcomes.

Results: Of 103 eligible participants, 87 were enrolled ( = 40, control  = 47; mean 57.6y [SD = 12.3], 44.8% female). Retention was ≥95% across arms. There were no significant differences in TEQ scores. participants engaged with the app on 62.9% of trial days. PAP use was high across both arms ( vs. Control: mean hours 5.98 vs. 5.86). There were no differences in PAP adherence or clinical outcomes.

Conclusions: was feasible and acceptable among PAP-naive patients with OSA.

Clinical Trial Registration: NCT03156283https://www.clinicaltrials.gov/study/NCT03156283.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11136882PMC
http://dx.doi.org/10.1080/15402002.2023.2289442DOI Listing

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